Incidental Mutation 'IGL00915:Srp72'
| ID |
27407 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Srp72
|
| Ensembl Gene |
ENSMUSG00000036323 |
| Gene Name |
signal recognition particle 72 |
| Synonyms |
5730576P14Rik, 72kDa |
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.947)
|
| Stock # |
IGL00915
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
5 |
| Chromosomal Location |
77122548-77147782 bp(+) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
C to A
at 77126460 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Cysteine to Stop codon
at position 87
(C87*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000113312
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000101087]
[ENSMUST00000120550]
|
| AlphaFold |
F8VQC1 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000101087
AA Change: C87*
|
| SMART Domains |
Protein: ENSMUSP00000098648
Gene: ENSMUSG00000036323
AA Change: C87*
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
3 |
11 |
N/A |
INTRINSIC |
|
Pfam:TPR_9
|
19 |
70 |
2.7e-2 |
PFAM |
|
Pfam:SRP_TPR_like
|
30 |
157 |
5.5e-25 |
PFAM |
|
Pfam:TPR_8
|
176 |
208 |
2.3e-3 |
PFAM |
|
Pfam:TPR_1
|
226 |
259 |
2.4e-4 |
PFAM |
|
Pfam:TPR_2
|
226 |
259 |
4.9e-5 |
PFAM |
|
Pfam:TPR_8
|
226 |
259 |
1.1e-2 |
PFAM |
|
Pfam:TPR_9
|
412 |
490 |
1.3e-3 |
PFAM |
|
Pfam:SRP72
|
531 |
588 |
6.2e-26 |
PFAM |
|
low complexity region
|
630 |
639 |
N/A |
INTRINSIC |
|
low complexity region
|
647 |
668 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000120550
AA Change: C87*
|
| SMART Domains |
Protein: ENSMUSP00000113312
Gene: ENSMUSG00000036323
AA Change: C87*
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
3 |
11 |
N/A |
INTRINSIC |
|
Pfam:TPR_9
|
19 |
72 |
2.5e-2 |
PFAM |
|
Blast:TPR
|
109 |
142 |
2e-11 |
BLAST |
|
Blast:TPR
|
176 |
209 |
5e-10 |
BLAST |
|
Pfam:TPR_6
|
280 |
310 |
2.5e-3 |
PFAM |
|
Pfam:TPR_9
|
351 |
429 |
1.4e-3 |
PFAM |
|
Pfam:SRP72
|
465 |
527 |
5.8e-24 |
PFAM |
|
low complexity region
|
569 |
578 |
N/A |
INTRINSIC |
|
low complexity region
|
586 |
607 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000148423
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000150661
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes the 72 kDa subunit of the signal recognition particle (SRP), a ribonucleoprotein complex that mediates the targeting of secretory proteins to the endoplasmic reticulum (ER). The SRP complex consists of a 7S RNA and 6 protein subunits: SRP9, SRP14, SRP19, SRP54, SRP68, and SRP72, that are bound to the 7S RNA as monomers or heterodimers. SRP has at least 3 distinct functions that can be associated with the protein subunits: signal recognition, translational arrest, and ER membrane targeting by interaction with the docking protein. Mutations in this gene are associated with familial bone marrow failure. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2012]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 25 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca3 |
T |
A |
17: 24,593,220 (GRCm39) |
Y206N |
probably damaging |
Het |
| Aebp2 |
A |
G |
6: 140,587,980 (GRCm39) |
N350S |
probably benign |
Het |
| Cerkl |
A |
G |
2: 79,171,843 (GRCm39) |
S367P |
probably benign |
Het |
| Ddx60 |
T |
G |
8: 62,440,465 (GRCm39) |
V1039G |
possibly damaging |
Het |
| Fstl4 |
A |
T |
11: 53,067,825 (GRCm39) |
M563L |
probably benign |
Het |
| Fzd9 |
C |
T |
5: 135,278,323 (GRCm39) |
V521M |
probably damaging |
Het |
| Gorab |
C |
T |
1: 163,224,426 (GRCm39) |
R125Q |
probably benign |
Het |
| Macc1 |
G |
A |
12: 119,410,749 (GRCm39) |
D506N |
probably benign |
Het |
| Mettl17 |
C |
A |
14: 52,124,746 (GRCm39) |
F119L |
probably benign |
Het |
| Nbas |
C |
A |
12: 13,424,753 (GRCm39) |
C997* |
probably null |
Het |
| Neil1 |
A |
G |
9: 57,051,261 (GRCm39) |
|
probably null |
Het |
| Or2r11 |
A |
G |
6: 42,437,884 (GRCm39) |
I23T |
probably benign |
Het |
| Prune2 |
A |
G |
19: 16,993,617 (GRCm39) |
E185G |
probably damaging |
Het |
| Ralgapa2 |
A |
G |
2: 146,184,442 (GRCm39) |
S1522P |
probably damaging |
Het |
| Scd1 |
A |
G |
19: 44,388,796 (GRCm39) |
L218P |
possibly damaging |
Het |
| Setdb1 |
A |
T |
3: 95,254,099 (GRCm39) |
F234L |
probably damaging |
Het |
| Sos1 |
A |
G |
17: 80,741,367 (GRCm39) |
S473P |
probably benign |
Het |
| Spata31d1a |
T |
C |
13: 59,849,999 (GRCm39) |
S710G |
probably benign |
Het |
| Tas2r126 |
T |
A |
6: 42,412,283 (GRCm39) |
I272K |
possibly damaging |
Het |
| Trim38 |
A |
T |
13: 23,975,015 (GRCm39) |
Y318F |
possibly damaging |
Het |
| Trnt1 |
A |
G |
6: 106,756,387 (GRCm39) |
K433E |
probably benign |
Het |
| Umodl1 |
A |
G |
17: 31,227,724 (GRCm39) |
|
probably benign |
Het |
| Urb1 |
A |
G |
16: 90,575,986 (GRCm39) |
F857L |
possibly damaging |
Het |
| Vps45 |
A |
G |
3: 95,953,662 (GRCm39) |
|
probably null |
Het |
| Zfhx4 |
A |
T |
3: 5,310,583 (GRCm39) |
I989F |
probably damaging |
Het |
|
| Other mutations in Srp72 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00473:Srp72
|
APN |
5 |
77,132,023 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02731:Srp72
|
APN |
5 |
77,142,062 (GRCm39) |
missense |
probably damaging |
0.98 |
|
PIT4468001:Srp72
|
UTSW |
5 |
77,142,053 (GRCm39) |
missense |
probably benign |
|
|
R0009:Srp72
|
UTSW |
5 |
77,135,732 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0318:Srp72
|
UTSW |
5 |
77,132,047 (GRCm39) |
missense |
probably benign |
0.27 |
|
R1645:Srp72
|
UTSW |
5 |
77,146,125 (GRCm39) |
missense |
probably benign |
0.05 |
|
R1678:Srp72
|
UTSW |
5 |
77,128,154 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1682:Srp72
|
UTSW |
5 |
77,135,717 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R2037:Srp72
|
UTSW |
5 |
77,124,338 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2364:Srp72
|
UTSW |
5 |
77,132,209 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2876:Srp72
|
UTSW |
5 |
77,143,767 (GRCm39) |
splice site |
probably benign |
|
|
R4072:Srp72
|
UTSW |
5 |
77,146,098 (GRCm39) |
missense |
probably benign |
0.24 |
|
R4073:Srp72
|
UTSW |
5 |
77,146,098 (GRCm39) |
missense |
probably benign |
0.24 |
|
R4074:Srp72
|
UTSW |
5 |
77,146,098 (GRCm39) |
missense |
probably benign |
0.24 |
|
R4638:Srp72
|
UTSW |
5 |
77,138,142 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4803:Srp72
|
UTSW |
5 |
77,132,231 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R4864:Srp72
|
UTSW |
5 |
77,132,009 (GRCm39) |
missense |
probably benign |
0.35 |
|
R5188:Srp72
|
UTSW |
5 |
77,122,598 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R5217:Srp72
|
UTSW |
5 |
77,128,375 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5459:Srp72
|
UTSW |
5 |
77,132,185 (GRCm39) |
missense |
probably benign |
0.16 |
|
R5616:Srp72
|
UTSW |
5 |
77,135,781 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6460:Srp72
|
UTSW |
5 |
77,135,838 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6595:Srp72
|
UTSW |
5 |
77,132,047 (GRCm39) |
missense |
probably benign |
0.27 |
|
R6959:Srp72
|
UTSW |
5 |
77,142,070 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R6986:Srp72
|
UTSW |
5 |
77,142,723 (GRCm39) |
missense |
probably benign |
0.16 |
|
R7674:Srp72
|
UTSW |
5 |
77,122,673 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8729:Srp72
|
UTSW |
5 |
77,142,005 (GRCm39) |
missense |
probably benign |
0.11 |
|
R9402:Srp72
|
UTSW |
5 |
77,124,329 (GRCm39) |
nonsense |
probably null |
|
|
R9533:Srp72
|
UTSW |
5 |
77,128,274 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1177:Srp72
|
UTSW |
5 |
77,146,200 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2013-04-17 |
Incidental Mutation